Canonical Allele Identifier: CA507308063

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223348T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732447T>C , CM000681.2:g.35732447T>C	GRCh38
NC_000019.9:g.36223348T>C , CM000681.1:g.36223348T>C	GRCh37
NC_000019.8:g.40915188T>C	NCBI36
NG_052906.1:g.19429T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.204T>C
ENST00000673918.2:c.5832T>C	ENSP00000501283.1:p.Ser1944=
ENST00000674114.2:c.3439T>C	ENSP00000501039.2:n.3439T>C
ENST00000684977.1:c.1116T>C	ENSP00000509384.1:p.Ser372=
ENST00000689544.1:n.1051T>C
ENST00000691421.1:c.1119T>C	ENSP00000508674.1:p.Ser373=
ENST00000691855.1:c.5440T>C
ENST00000692961.1:c.5898T>C	ENSP00000509289.1:p.Ser1966=
ENST00000693677.1:c.704+118T>C	ENSP00000509779.1:n.704+118T>C
ENST00000420124.4:c.5898T>C MANE Select	ENSP00000398837.2:p.Ser1966=
ENST00000673918.1:c.5832T>C	ENSP00000501283.1:p.Ser1944=
ENST00000674114.1:c.3220T>C
ENST00000420124.2:c.5898T>C	ENSP00000398837.1:p.Ser1966=
NM_014727.2:c.5898T>C	NP_055542.1:p.Ser1966=
XM_011527561.1:c.5832T>C	XP_011525863.1:p.Ser1944=
XM_011527562.1:c.5898T>C	XP_011525864.1:p.Ser1966=
XM_011527563.1:c.5622T>C	XP_011525865.1:p.Ser1874=
XM_011527561.2:c.5334T>C	XP_011525863.2:p.Ser1778=
XM_011527562.2:c.5898T>C	XP_011525864.1:p.Ser1966=
XM_017027544.1:c.5898T>C	XP_016883033.1:p.Ser1966=
XM_017027545.1:c.5334T>C	XP_016883034.1:p.Ser1778=
XM_017027546.1:c.2862T>C	XP_016883035.1:p.Ser954=
NM_014727.3:c.5898T>C MANE Select	NP_055542.1:p.Ser1966=